Stickler Syndrome

Sponsored diagnostic testing programs for Stickler Syndrome

Stickler syndrome is a connective tissue disorder featuring retinal detachment risk, high myopia, hearing loss, joint hypermobility, and midface hypoplasia. Severity varies across individuals and subtypes. Genetic testing identifies the subtype and guides surveillance for vision, hearing, and orthopedic complications.

1 program found for Stickler Syndrome

Programs

1 program
Invitae Unlock™

Invitae Inherited Retinal Disorders Panel

This program offers U.S. clinicians access to comprehensive genetic testing for patients with suspected inherited retinal diseases, including RP, CRD, LCA, Stargardt disease, and other IRDs. Testing is also appropriate for asymptomatic individuals with a family history of IRD or a known pathogenic variant in a relevant gene, supporting diagnosis, risk assessment, and patient management.

Ophthalmology